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721840000: Hyperuricemia, anemia, renal failure syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3326212015 Hyperuricemia, anemia, renal failure syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3326213013 Hyperuricemia, anemia, renal failure syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3326214019 Hyperuricaemia, anaemia, renal failure syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3326215018 Familial juvenile hyperuricemic nephropathy type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3326216017 Familial juvenile hyperuricaemic nephropathy type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3326217014 Renin associated familial juvenile hyperuricemic nephropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3326218016 Renin associated familial juvenile hyperuricaemic nephropathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3326219012 A rare autosomal dominantly inherited disease of childhood characterized by hypoproliferative anemia, hyperuricemia and slowly progressing kidney failure due to dysregulation of the renin-angiotensin system. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3326220018 A rare autosomal dominantly inherited disease of childhood characterised by hypoproliferative anaemia, hyperuricaemia and slowly progressing kidney failure due to dysregulation of the renin-angiotensin system. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperuricemia, anemia, renal failure syndrome (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Hyperuricemia, anemia, renal failure syndrome (disorder) Is a Hyperuricemia true Inferred relationship Some
Hyperuricemia, anemia, renal failure syndrome (disorder) Is a Renal tubular disorder true Inferred relationship Some
Hyperuricemia, anemia, renal failure syndrome (disorder) Is a Urate nephropathy true Inferred relationship Some
Hyperuricemia, anemia, renal failure syndrome (disorder) Is a Hereditary nephropathy (disorder) true Inferred relationship Some
Hyperuricemia, anemia, renal failure syndrome (disorder) Finding site Renal tubule structure (body structure) true Inferred relationship Some 1
Hyperuricemia, anemia, renal failure syndrome (disorder) Finding site Kidney structure false Inferred relationship Some 2
Hyperuricemia, anemia, renal failure syndrome (disorder) Causative agent Urate false Inferred relationship Some 2
Hyperuricemia, anemia, renal failure syndrome (disorder) Causative agent Urate true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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